Allele Registry

Canonical Allele Identifier: PA658681480

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000572899

RCV000797361

ClinVar Variation:

479921

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Lys1296Gln	CA072260 NM_000179.3:c.3886A>C